3-amino-4-(4-methoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide

Base Information

Chemical Name:3-amino-4-(4-methoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide
CAS No.:720676-68-6
Molecular Formula:C₂₅H₂₃N₃O₂S
Molecular Weight:429.543
Hs Code.:
Mol file:720676-68-6.mol

Synonyms:3-amino-4-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-thieno[2,3-b]quinoline-2-carboxylic acid phenylamide

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Chemical Property of 3-amino-4-(4-methoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide

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Technology Process of 3-amino-4-(4-methoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide

There total 4 articles about 3-amino-4-(4-methoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: 720676-74-4
2-[3-cyano-4-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-quinolin-2-ylsulfanyl]-N-phenyl-acetamide

: 720676-68-6
3-amino-4-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-thieno[2,3-b]quinoline-2-carboxylic acid phenylamide

Guidance literature:: With sodium ethanolate; In ethanol; for 0.0833333h; Heating;
DOI:10.1002/jccs.200500136

Reference yield:

: 117601-23-7
4-(4-methoxyphenyl)-2-sulfanylidene-1,2,5,6,7,8-hexahydroquinoline-3-carbonitrile

: 720676-68-6
3-amino-4-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-thieno[2,3-b]quinoline-2-carboxylic acid phenylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / sodium acetate trihydrate / ethanol / 2 h / Heating

2: 93 percent / sodium ethanolate / ethanol / 0.08 h / Heating

With sodium ethanolate; sodium acetate; In ethanol; 2: Thorpe-Ziegler cyclisation;
DOI:10.1002/jccs.200500136

Reference yield:

: 587-65-5
N-chloroacetyl-aniline

: 720676-68-6
3-amino-4-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-thieno[2,3-b]quinoline-2-carboxylic acid phenylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / sodium acetate trihydrate / ethanol / 2 h / Heating

2: 93 percent / sodium ethanolate / ethanol / 0.08 h / Heating

With sodium ethanolate; sodium acetate; In ethanol; 2: Thorpe-Ziegler cyclisation;
DOI:10.1002/jccs.200500136